Search results for "monomer"
showing 10 items of 857 documents
Polypyrrole films functionalized with pendant titanocene dichloride complexes: Ellipsometric study of the electropolymerization process
2007
Electrochemical and ellipsometric methods have been used to study the electropolymerization process of a functionalized monomer, Tc3Py (in which pyrrole is covalently bonded with titanocene dichloride complex) on platinum electrode from a dilute monomer solution in acetonitrile. The deposition has been performed in the potentiodynamic regime. A new method for the acquisition and treatment of ellipsometric data has been proposed which allowed us to analyze the evolution of the film properties at each potential. The model of a single uniform layer was unable to describe the ellipsometric experimental observations with the necessary precision. A proper fitting of the data has been achieved con…
Electronic structure of phthalocyanines : Theoretical investigation of the optical properties of phthalocyanine monomers, dimers, and crystals
1990
We present valence effective Hamiltonian (VEH) calculations on the optical absorptions of a series of phthalocyanine compounds: the metal‐free phthalocyanine molecule, a model system for the lithium phthalocyanine molecule, the metal‐free phthalocyanine dimer, and model systems for the lutetium diphthalocyanine and the lithium phthalocyanine crystal. For these compounds, it is found that the major factor influencing the evolution of the optical transitions is not the electronic structure of the metal but rather the geometric structure: phthalocyanine intraring geometry and, in the dimers and crystals, interring separation and staggering angle. The origin of the so‐called Soret or B absorpti…
Investigation of molecular dimers by ensemble and single molecule spectroscopy
2002
International audience; We have investigated molecular dimers with different electronic coupling strengths by bulk and single molecule spectroscopy. In one of the dimers the two monomers (perylene-monoimide) are directly connected via a single bond while in the other one they are separated by the benzil motif. The close proximity of the monomers in the first case gives rise to excitonic band splitting which is clearly observable in the bulk absorption spectra. For the benzil structure the electronic interactions are governed by Förster-type energy hopping between the monomers. Fluorescence intensity trajectories at the single molecule level show one-step and two-step bleaching behaviour whi…
Anionic Polymerization of (Meth)acrylates in the Presence of Cesium Halide−Trialkylaluminum Complexes in Toluene
2001
The polymerization of methyl methacrylate and various acrylates initiated by ester enolates in the presence of cesium halide-trialkylaluminum complexes, Cs[Al n R 2n X] (n = 1, 2; R = Et, Bu'), in toluene has living and controlled character at -20 °C for methacrylates (X = Cl) and at -65 °C for n-butyl acrylate (X = F). Quantitative monomer conversions are usually reached, leading to polymers with narrow molecular weight distributions (M w /M n < 1.1). Kinetic investigations indicate a rather complex polymerization mechanism, and we assume an equilibrium between at least two active species. With this new initiating system, beside acrylate homopolymers, random and graft copolymers can be syn…
Characterization of sulfobetaine monomers by nuclear magnetic resonance spectroscopy: a note
1995
A set of zwitterionic monomers bearing the 3-ammoniopropanesulfonate moiety is analysed in CDCl3, CD3OD and D2O by one- and two-dimensional H-1 n.m.r. and C-13 n.m.r. spectroscopy. Absolute and relative positions of the n.m.r, signals are determined depending on the solvent used; the refined assignments of the signals in the vicinity of the ammonium group deviate from previously proposed assignments based on standard n.m.r, shift tables. Still, there is no convincing evidence for a special ring current effect due to a six-membered ring conformation of the betaine moiety.
Polymerizable and polymeric zwitterionic surfactants: 2. Surface activity and aggregation behaviour in aqueous systems
1991
Abstract The surfactant properties of a series of permanently zwitterionic monomers and polymers were studied with respect to structural variations. A strong influence of the molecular geometry on solubility and aggregation behaviour was observed, in particular for the polymers. Whereas all monomers were water-soluble and true surfactants, the water solubility of the polymers was restricted to selected geometries. Water-soluble polymers showed the properties of classical polysoaps, i.e. low surface activity and solubilization power for hydrophobic solutes. In contrast, water-insoluble polymers formed stable monolayers at the air-water interface and could be deposited onto solid substrates b…
Molecular Recognition by Hydrogen Bonding in Polyelectrolyte Multilayers
1997
Functional polyanions were prepared by copolymerization of sulfopropyl acrylate and sulfopropyl methacrylate with monomers bearing triaminopyrimidine or barbituric acid functionalities, respectively. Functionalized polyelectrolyte multilayers were assembled from these copolymers by stepwise alternating adsorption with poly(choline methacrylate). These multilayers are suited for molecular recognition of substrates that are complementary to the functional groups incorporated. Thus, multilayers containing triaminopyrimidine moieties selectively bind barbituric acid, and vice versa, when exposed to solutions of the 1:1 complex of barbituric acid and triaminopyrimidine. The molecular recognition…
Poly(ethylene oxide)-block-poly(n-butyl acrylate)-block-poly(acrylic acid) triblock terpolymers with highly asymmetric hydrophilic blocks: synthesis …
2013
The synthesis and aggregation behaviour in aqueous media of novel amphiphilic poly(ethylene oxide)-block-poly(n-butyl acrylate)-block-poly(acrylic acid) (PEO–PnBA–PAA) triblock terpolymers were studied. Terpolymers composed of two highly asymmetric hydrophilic PEO (113 monomer units) and PAA (10–17 units) blocks, and a longer soft hydrophobic PnBA block (163 or 223 units) were synthesized by atom transfer radical polymerisation (ATRP) of n-butyl acrylate and tert-butyl acrylate (tBA), followed by selective hydrolysis of the PtBA blocks. These terpolymers are not directly soluble in water but form defined spherical micelles by employing the dialysis method as confirmed by dynamic light scatt…
Modified arabinoxylan-based films
2004
Abstract Oxygen plasma and electron beam irradiation were used to graft hydrophobic substances and by this way, to reduce water vapor permeability (WVP) of arabinoxylan-based (AX-based) films. Stearyl acrylate (SA) and stearyl methacrylate (SM) were used as reactive monomers. The homogeneous AX-based films, which were pre-activated by oxygen plasma and impregnated with a solution of SA before being exposed to an electron beam (EB), had contact angles that increased from 71° (untreated films) to 122° (treated films). A decrease of about 24% in the WVP was obtained and new chemical groupings were observed on the FTIR spectra of these films. Acrylate monomers were also dispersed into the arabi…
Copolymerization of n-Butyl Acrylate with Methyl Methacrylate and PMMA Macromonomers: Comparison of Reactivity Ratios in Conventional and Atom Trans…
1999
The reactivity ratios of n-butyl acrylate (nBuA) with methyl methacrylate (MMA) and ω-methacryloyl-PMMA macromonomers (MM) in conventional and atom transfer radical copolymerization (ATRP) have been determined. For the copolymerization of nBuA with MMA, good agreement of the ratios is observed between conventional and controlled radical copolymerization, indicating that chemoselectivities in both processes are similar. The relative reactivity of the MM (1/rnBuA) in conventional copolymerization is significantly lower than that of MMA. It depends on the concentration of the comonomers but is not significantly influenced by the length of the MM. At high concentrations the relative reactivity …